蛋白质分离纯化新技术和技术要点
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  • 蛋白质分离纯化新技术和技术要点

  • 点击:    作者:   来源:诺贝尔学术论坛 日期:2008-01-14    本站论坛
3. 检测器中充满缓冲液,看记录笔的位置,最好接近~10%刻度的地方,这样防止出现吸光度值低于缓冲液无法记录的情况;如果笔位太高,应增大检测器信号输出,重新按步骤2 调节;反之降低信号输出;有的记录仪也可调节输入信号的范围,这样子就更方便了。满刻度的调节要视具体应用,不一定是1mg/ml 的蛋白浓度。

9about dimension of column:davidzrock W/~- A8

"The choice of inner diameter may be based on the desired sample load or on considerations of the extra XS<Sp,v]

dispersion |~F}tjQs

effects from the wall region,which extends 20 particle diameters away from the wall. ... The length of the column p$5*Pp

is primarily chosen according to the resolution that is required." KHCa23ypw

"The dimensions may be chosen according to the application at hand, but most laboratory columns have a 4- to $W#_YMax

16-mm inner diameter(i.d.) and a length of 25 to 70 cm." 1?%n&jg *

-----From ‘Protein Purification principles,High Resolution Methods,and Applications’ 2ed edited by J.C. Janson (hx8rf6j>}

and L.Ryden P(qV70GWJ1

"The resolution of two separated zones in gel filtration increases as the sequare root of column length. Long LQDgyp*9

columns should,therefore,be used to obtain the best resolution in analytical fractionation. Bed heights of greater P#"m9A

than 1m are seldom required. If a very long bed is judged to be necessary ,the effective bed height can often be ZqH>U}Jd

increased simply by recycling or by using columns coupled in series."

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